Canonical Allele Identifier: CA2322525642

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631261T= , CM000681.2:g.10631261T=	GRCh38
NC_000019.9:g.10741937T= , CM000681.1:g.10741937T=	GRCh37
NC_000019.8:g.10602937T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.331-14T= MANE Select	ENSP00000336888.4:n.331-14T=
ENST00000335757.9:c.331-14T=	ENSP00000336888.4:n.331-14T=
ENST00000407327.8:c.325-14T=	ENSP00000385135.3:n.325-14T=
ENST00000586078.5:c.331-14T=	ENSP00000466664.1:n.331-14T=
ENST00000588409.1:c.245+3257T=	ENSP00000468070.1:n.245+3257T=
ENST00000588465.5:n.240-14T=
ENST00000588688.5:c.172-14T=	ENSP00000467552.1:n.172-14T=
ENST00000590382.5:c.166-14T=	ENSP00000468691.1:n.166-14T=
ENST00000590857.5:c.-219-14T=	ENSP00000465547.1:n.-219-14T=
ENST00000592293.5:c.*128-14T=	ENSP00000466612.1:n.*128-14T=
NM_001145056.1:c.325-14T=	NP_001138528.1:n.325-14T=
NM_020428.3:c.331-14T=	NP_065161.3:n.331-14T=
XM_005259997.1:c.331-14T=	XP_005260054.1:n.331-14T=
XM_005259999.1:c.325-14T=	XP_005260056.1:n.325-14T=
NM_001363611.1:c.331-14T=	NP_001350540.1:n.331-14T=
XM_005259999.2:c.325-14T=	XP_005260056.1:n.325-14T=
NM_020428.4:c.331-14T= MANE Select	NP_065161.3:n.331-14T=
NM_001145056.2:c.325-14T=	NP_001138528.1:n.325-14T=
NM_001363611.2:c.331-14T=	NP_001350540.1:n.331-14T=